Species

KNApSAcK Entry

Organism name Pterocaulon alopecuroides
Genus Pterocaulon
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pterocaulon
Linked NCBI taxonomy ID 81513
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (3)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00008636 External link 512 7-O-Prenyltaxifolin
No. 276 No. 14
C00019845 External link 512 7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-5-methoxycoumarin
CHEMBL1574904
8 / 9 / 7 No. 579 No. 25
C00019846 External link 512 7-(2,3-Dihydroxy-3-methylbutyloxy)-5-hydroxy-6-methoxycoumarin
No. 579 No. 25

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00019845 0 / 0
P04062 Glucosylceramidase Enzyme C00019845 6 / 4
P17405 Sphingomyelin phosphodiesterase Enzyme C00019845 2 / 2
P06280 Alpha-galactosidase A Enzyme C00019845 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00019845 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00019845 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00019845 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00019845 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#301500 Fabry disease P06280
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#168600 Parkinson disease, late-onset; pd P04062

KEGG DISEASE (7)

KEGG name UniProt
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00125 Fabry disease P06280 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)